Canonical Allele Identifier: CA915941159
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 656223
ClinVar RCV Id: RCV000812587 RCV003307514
dbSNP Id: rs1570958038
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044817_17044818dup , CM000663.2:g.17044817_17044818dup GRCh38
NC_000001.10:g.17371312_17371313dup , CM000663.1:g.17371312_17371313dup GRCh37
NC_000001.9:g.17243899_17243900dup NCBI36
NG_012340.1:g.14353_14354dup , LRG_316:g.14353_14354dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-29_-28dup ENSP00000481376.2:n.-29_-28dup
ENST00000491274.6:c.101_102dup ENSP00000480482.2:p.Pro35ThrfsTer29
ENST00000375499.8:c.143_144dup MANE Select ENSP00000364649.3:p.Pro49ThrfsTer29
ENST00000375499.7:c.143_144dup ENSP00000364649.3:p.Pro49ThrfsTer29
ENST00000463045.2:c.-29_-28dup ENSP00000481376.1:n.-29_-28dup
ENST00000466613.2:n.155_156dup
ENST00000475506.1:n.60_61dup
ENST00000485515.5:n.131_132dup
ENST00000491274.5:c.101_102dup ENSP00000480482.1:p.Pro35ThrfsTer29
NM_003000.2:c.143_144dup , LRG_316t1:c.143_144dup NP_002991.2:p.Pro49ThrfsTer29
NM_003000.3:c.143_144dup MANE Select NP_002991.2:p.Pro49ThrfsTer29
Search 100 bp 5'
Search 100 bp 3'